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NCT06376773

Neoadjuvant Treatment Based on Gastric Cancer Molecular Subtyping.

Completed Last updated 19 April 2024
What this trial tests

trial testing combination chemotherapy with Apatinib or Camrelizumab in Advanced Gastric Cancer in 234 participants. Completed in 30 November 2023.

Timeline
1 June 2022
Primary endpoint
1 July 2023
30 November 2023

Quick facts

Lead sponsorFujian Medical University
StatusCompleted
Study typeOBSERVATIONAL
Enrollment234
Start date1 June 2022
Primary completion1 July 2023
Estimated completion30 November 2023
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Fujian Medical University

Who can join

Adults 18 to 80, any sex, with Advanced Gastric Cancer or Neoadjuvant Therapy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Extensive research employing diverse omics methodologies has unveiled a varied landscape of gastric cancer (GC). Recent progress in next-generation sequencing and other genomic technologies has facilitated a more intricate exploration of GC at the molecular level. This study aimed to identify the most effective drug therapeutics for patients with the mesenchymal subtype of gastric cancer.Based on RNA-seq transcriptome, 234 patients were divided into four molecular subtypes: mesenchymal, immunogenic, metabolic, and classic.Our analysis has revealed that, for neoadjuvant therapy in advanced gastric cancer (AGC), the mesenchymal subtype stands out as the ideal patient population benefiting from Apatinib, without a concurrent increase in postoperative complications.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Advanced Gastric Cancer

Currently open trials in the same condition.

Other Fujian Medical University trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06376773.

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